Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 22nd May 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 98, 2016
Previous Article Next Article

Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes

Author affiliations

Abstract

Gold(I) catalyzes domino homodimerization of o-alkynylbenzaldehydes via a sequence of 6-endo-dig-cyclization, amine addition, and [4+2] cycloaddition involving two bicyclic intermediates. The resulting products integrate medicinally relevant 1,2-dihydronaphthalene and isochromene moieties into a single amine-substituted tetracyclic framework.

Graphical abstract: Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes

Back to tab navigation

Supplementary files

Publication details

The article was received on 08 Oct 2016, accepted on 15 Nov 2016 and first published on 15 Nov 2016


Article type: Communication
DOI: 10.1039/C6CC08132K
Chem. Commun., 2016,52, 14133-14136

  •   Request permissions

    Tetracyclic dihydronaphthalene derivatives via gold-catalyzed aminative homodimerization of ortho-alkynylbenzaldehydes

    A. A. Ruch, F. Kong, V. N. Nesterov and L. M. Slaughter, Chem. Commun., 2016, 52, 14133
    DOI: 10.1039/C6CC08132K

Search articles by author

Spotlight

Advertisements